Inherited Skin Disorders tests in Dubai & UAE

Compare available Inherited Skin Disorders tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

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Listed price range

2,800.00 AED

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Inherited Skin Disorders test prices

Showing 1–5 of 5 matching tests.

Inherited Skin Disorders diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4991 ABCA12 Gene Sequencing (Harlequin Ichthyosis) Test This test analyzes the ABCA12 gene to detect mutations associated with Harlequin ichthyosis, a severe autosomal recessive skin disorder.	Peripheral Whole Blood (EDTA)	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ABCA12 gene sequence", "Pathogenic variants (missense, nonsense, frameshift, splice-site, indels)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of recent blood transfusions (within 4 weeks) or bone marrow/stem cell transplant (within 12 months)"] Indications ["Suspected Harlequin ichthyosis", "Carrier screening in at-risk individuals", "Prenatal diagnosis in families with known mutations"] Measurement technique Confirm with laboratory Codes LOINC: 81409-9 ICD-10: Q80.4 Clinical summary This test analyzes the ABCA12 gene to detect mutations associated with Harlequin ichthyosis, a severe autosomal recessive skin disorder.
TEST-4457 DDB2 Gene Xeroderma Pigmentosum Group E Genetic Test This genetic test analyzes the DDB2 gene to identify mutations causing Xeroderma Pigmentosum Group E.	Whole Blood (FTA card or 3 mL EDTA tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the DDB2 gene", "Sensitivity to UV radiation"] Parameters [] Preparation ["No fasting required"] Indications ["Diagnosis of Xeroderma Pigmentosum Group E", "Family screening for XP-E", "Assessment of cancer predisposition related to DDB2 mutations", "Carrier screening for couples planning pregnancy"] Measurement technique Confirm with laboratory Codes LOINC: 96515-6 ICD-10: Q82.1 Clinical summary This genetic test analyzes the DDB2 gene to identify mutations causing Xeroderma Pigmentosum Group E.
TEST-5087 GJB4 Gene Erythrokeratodermia Variabilis et Progressiva (EKVP) Genetic Test This genetic test evaluates the GJB4 gene for pathogenic variants associated with Erythrokeratodermia Variabilis et Progressiva (EKVP).	Whole Blood or Buccal Swab	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GJB4 gene sequence", "Pathogenic variants in GJB4"] Parameters [] Preparation ["No fasting is required.", "Continue all regular medications unless instructed otherwise by your doctor."] Indications ["Suspected clinical diagnosis of Erythrokeratodermia Variabilis et Progressiva (EKVP)", "Genetic counselling for families with EKVP"] Measurement technique Confirm with laboratory Codes LOINC: 82941-3 ICD-10: Q82.8, Z84.89, Z13.79 Clinical summary This genetic test evaluates the GJB4 gene for pathogenic variants associated with Erythrokeratodermia Variabilis et Progressiva (EKVP).
TEST-5108 LAMB3 Gene Sequencing (NGS) Test This test identifies genetic mutations in the LAMB3 gene associated with Junctional Epidermolysis Bullosa, Herlitz type.	Peripheral whole blood (EDTA tube) or DNA FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LAMB3 gene coding exons", "LAMB3 gene flanking splice-site regions"] Parameters [] Preparation ["No fasting needed", "Ensure guardian signs informed consent form"] Indications ["Diagnostic confirmation in symptomatic infants", "Carrier testing in at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 81265-3 ICD-10: Q81.1 Clinical summary This test identifies genetic mutations in the LAMB3 gene associated with Junctional Epidermolysis Bullosa, Herlitz type.
TEST-4950 LIPN Gene Ichthyosis Lamellar Type 4 Genetic Test This test identifies pathogenic variants in the LIPN gene associated with lamellar ichthyosis type 4.	Whole Blood (EDTA) or FTA Card (Dried Blood Spot)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in LIPN gene", "Copy Number Variants (CNV) in LIPN gene"] Parameters [] Preparation [] Indications ["Suspected lamellar ichthyosis type 4", "Family history of ichthyosis", "Need for genetic confirmation for management and counseling"] Measurement technique Confirm with laboratory Codes LOINC: 81261-6 ICD-10: Q80.2 Clinical summary This test identifies pathogenic variants in the LIPN gene associated with lamellar ichthyosis type 4.

Category overview

Inherited Skin Disorders: overview

Enduring severe blistering, extreme scaling, or dangerous pigmentation issues from birth requires specialized diagnostic insights to protect your skin's foundational barrier and prevent severe complications. Representing an advanced subspecialty within our Genetics department, testing for Inherited Skin Disorders evaluates your DNA for inherited mutations that disrupt the structural proteins, keratin production, or melanin synthesis of your skin. By leveraging state-of-the-art diagnostic technology, this precise molecular screening helps confirm rare genodermatoses like epidermolysis bullosa, ichthyosis, or albinism, providing the definitive data necessary to safely guide highly personalized wound care protocols, preventative dermatological strategies, and specialized clinical oversight. Recognized for clinical rigor among premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, unparalleled diagnostic precision, and incredibly prompt reporting. Protect your dermatological wellness—book your inherited skin disorders testing in UAE, arrange a secure home sample collection, or consult our expert medical professionals.

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